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DiMauro

Showing results (401-410 of 942) with videos related to

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Biochemical and Biophysical Research Communications|September 23, 1997
Identification of a novel mutation in the mtDNA ND5 gene associated with MELASF M Santorelli, K Tanji, R Kulikova, et al.
Neurology|June 20, 1998
A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intoleranceJ Vissing, M B Salamon, P Arlien-Søborg, et al.
Free Radical Biology & Medicine|December 13, 2006
Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcriptMansour Alemi, Alessandro Prigione, Alice Wong, et al.
Neurology|January 28, 2004
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafnessM Mancuso, M Filosto, M Bellan, et al.
Journal of Animal Physiology and Animal Nutrition|March 24, 2016
Different physical forms of one diet fed to growing pigs induce morphological changes in mandubular glands and local leptin (Ob) production and receptor (ObR) expressionM G Cappai, C Dall'Aglio, S J Sander, et al.
Surgery|June 1, 1986
Carnitine metabolism during fasting in dogsJ Rodriguez, J Bruyns, J Askanazi, et al.
American Journal of Human Genetics|January 1, 1994
Three new mutations in patients with myophosphorylase deficiency (McArdle disease)S Tsujino, S Shanske, I Nonaka, et al.
Archives of Neurology|January 1, 1994
Dementia of adult polyglucosan body disease. Evidence of cortical and subcortical dysfunctionZ Rifai, M Klitzke, R Tawil, et al.
Archives of Neurology|October 22, 2003
Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genesMichelangelo Mancuso, Massimiliano Filosto, Seiichi Tsujino, et al.
American Journal of Medical Genetics|December 1, 1991
Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?C T Moraes, M Zeviani, E A Schon, et al.
Pageof 95

Showing results (401-410 of 942) with videos related to

Sort By:
Pageof 95
Biochemical and Biophysical Research Communications|September 23, 1997
Identification of a novel mutation in the mtDNA ND5 gene associated with MELASF M Santorelli, K Tanji, R Kulikova, et al.
Neurology|June 20, 1998
A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intoleranceJ Vissing, M B Salamon, P Arlien-Søborg, et al.
Free Radical Biology & Medicine|December 13, 2006
Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcriptMansour Alemi, Alessandro Prigione, Alice Wong, et al.
Neurology|January 28, 2004
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafnessM Mancuso, M Filosto, M Bellan, et al.
Journal of Animal Physiology and Animal Nutrition|March 24, 2016
Different physical forms of one diet fed to growing pigs induce morphological changes in mandubular glands and local leptin (Ob) production and receptor (ObR) expressionM G Cappai, C Dall'Aglio, S J Sander, et al.
Surgery|June 1, 1986
Carnitine metabolism during fasting in dogsJ Rodriguez, J Bruyns, J Askanazi, et al.
American Journal of Human Genetics|January 1, 1994
Three new mutations in patients with myophosphorylase deficiency (McArdle disease)S Tsujino, S Shanske, I Nonaka, et al.
Archives of Neurology|January 1, 1994
Dementia of adult polyglucosan body disease. Evidence of cortical and subcortical dysfunctionZ Rifai, M Klitzke, R Tawil, et al.
Archives of Neurology|October 22, 2003
Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genesMichelangelo Mancuso, Massimiliano Filosto, Seiichi Tsujino, et al.
American Journal of Medical Genetics|December 1, 1991
Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?C T Moraes, M Zeviani, E A Schon, et al.
Pageof 95